A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576125



Internal ID20949196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133293068..134631849hg38UCSC Ensembl
chr11:133162963..134501743hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381338782
hg191338781
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231116
Samples
Known GenesACAD8, B3GAT1, GLB1L2, GLB1L3, IGSF9B, JAM3, LOC100128239, LOC283177, MIR4697, MIR4697HG, NCAPD3, OPCML, SPATA19, THYN1, VPS26B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576125
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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